戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 68294作成日:2026年10月25日

Triethylamine → 6-(2-Methoxyphenyl)-2-(methylthio)pyrimidine-4-carboxamide

https://huagongshe.com/reaction/68294

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Ammonium ChlorideHCID 25517—
反応物PyBOPHCID 2724699—
反応物6-(2-Methoxyphenyl)-2-(methylthio)pyrimidine-4-carboxylic acidHCID 39375279—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物6-(2-Methoxyphenyl)-2-(methylthio)pyrimidine-4-carboxamideHCID 58872649—

反応手順

To a stirred suspension of 6-(2-methoxyphenyl)-2-(methylthio)pyrimidine-4-carboxylic acid (9.8 g, 40 mmol), triethylamine (33 mL, 240 mmol), and ammonium chloride (11 g, 200 mmol) in DMF (40 mL) was added PyBOP (21.9 g, 42 mmol) in five portions. The reaction was complete in 2 h, as determined by LCMS analysis. The reaction mixture was poured into water (1.5 L) and stirred for 10 minutes. The precipitate was collected by filtration and dried overnight under high vacuum to give 6-(2-methoxyphenyl)-2-(methylthio)pyrimidine-4-carboxamide. 1H NMR (300 MHz, CDCl3) δ 8.40 (s, 0.7H), 8.05 (m, 1.3H), 7.74 (bs, 1H), 7.44 (m, 1H), 7.05 (m, 2H), 5.78 (bs, 1H), 3.92 (s, 3H); 2.65 (s, 3H). HPLC ret. time 2.71 min, 10-100% CH3CN, 5 min gradient; ESI-MS m/z 245.9 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822451B2
出典データセットuspto-grants-2014_09
ORD IDord-de42c27c4d3f4307a5aa952636231542
出典メモuspto-grants-2014_09